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    Lefebvre, M., Bruel, A., Tisserant, E., Bourgon, N., Duffourd, Y., Collardeau-Frachon, S., Attie-Bitach, T., Kuentz, P., assoum, M., Schaefer, E., El Chehadeh, S., Antal, M. C., Kremer, V., Girard-Lemaitre, F., Mandel, J., Lehalle, D., Nambot, S., Jean-Marçais, N., Houcinat, N., Moutton, S., Marle, N., Lambert, L., Jonveaux, P., Foliguet, B., Mazutti, J., Gaillard, D., Alanio, E., Poirisier, C., Lebre, A., Aubert-Lenoir, M., Arbez-Gindre, F., Odent, S., Quélin, C., Loget, P., Fradin, M., Willems, M., Bigi, N., Perez, M., Blesson, S., Francannet, C., Beaufrere, A., Patrier-Sallebert, S., Guerrot, A., Goldenberg, A., Brehin, A., Lespinasse, J., Touraine, R., Capri, Y., Saint-Frison, M., Laurent, N., Philippe, C., Tran Mau-them, F., Thevenon, J., Faivre, L., Thauvin-Robinet, C., & Vitobello, A. (2021). genotype-first in a cohort of 95 fetuses with multiple congenital abnormalities: when exome sequencing reveals unexpected fetal phenotype-genotype correlations. Journal of medical genetics, 58(6), 400–413. http://access.bl.uk/ark:/81055/vdc_100130754655.0x000020
  
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